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rs741702

From SNPedia

Orientationplus
Stabilizedplus
Make rs741702(A;A)
Make rs741702(A;C)
Make rs741702(C;C)
ReferenceGRCh38 38.1/141
Chromosome19
Position12913436
GeneSYCE2
is asnp
is mentioned by
dbSNPrs741702
ebirs741702
HLIrs741702
Exacrs741702
Varsomers741702
Maprs741702
PheGenIrs741702
hapmaprs741702
1000 genomesrs741702
hgdprs741702
ensemblrs741702
gopubmedrs741702
geneviewrs741702
scholarrs741702
googlers741702
pharmgkbrs741702
gwascentralrs741702
openSNPrs741702
23andMers741702
23andMe allrs741702
SNP Nexus

SNPshotrs741702
SNPdbers741702
MSV3drs741702
GWAS Ctlgrs741702
GMAF0.2966
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23222517OA-icon.png]
Trait Red blood cell traits
Title Seventy-five genetic loci influencing the human red blood cell.
Risk Allele A
P-val 8E-20
Odds Ratio .01 [-0.00184-0.01384] unit increase